36155722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 126150528-G-A

36155722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 126150528-G-T

36155760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, undefined
orthologous variants: 126150480-G-A

36155760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, undefined
orthologous variants: 126150480-G-T

http://identifiers.org/hco/1/GRCh38#36155820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126150440-C-A

36155855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126150406-G-T

36155903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 126150359-C-T

36155930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150332-A-G

36155999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150263-G-A

36156013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 126150249-G-A

36156013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 126150249-G-T

http://identifiers.org/hco/1/GRCh38#36156054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126150213-C-A

36156054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150213-C-T

36156069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150201-G-A

36156069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150201-G-T

36156077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150193-G-A

36156077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150193-G-C

36156077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150193-G-T

36156090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150180-G-A

36156090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126150180-G-T

http://identifiers.org/hco/1/GRCh38#36156183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126150092-C-A

36156183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126150092-C-T

http://identifiers.org/hco/1/GRCh38#36156213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126150061-C-A

36156213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126150061-C-G

36156213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126150061-C-T

36156327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126149949-G-A

36156327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126149949-G-C

36156327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126149949-G-T

http://identifiers.org/hco/1/GRCh38#36156339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126149937-C-A

36156339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126149937-C-T

http://identifiers.org/hco/1/GRCh38#36156376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126149900-C-A

36156376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126149900-C-T

36156468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149803-G-A

36156468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149803-G-C

36156468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149803-G-T

36156474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149797-A-G

36156497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149773-G-A

36156497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149773-G-C

36156497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149773-G-T

36156502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149768-T-A

36156502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149768-T-C

36156502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149768-T-G

http://identifiers.org/hco/1/GRCh38#36156514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126149756-A-C

36156514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149756-A-G

36156514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149756-A-T

36156549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149722-G-A

36156549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149722-G-T

http://identifiers.org/hco/1/GRCh38#36156554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126149717-C-A

36156554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149717-C-T

36156790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126149477-C-T

36157088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149187-G-A

36157088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149187-G-C

36157088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149187-G-T

http://identifiers.org/hco/1/GRCh38#36157154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126149121-C-A

36157154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149121-C-G

36157178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126149097-T-C

36157345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148954-G-A

36157345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148954-G-T

http://identifiers.org/hco/1/GRCh38#36157371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126148920-C-A

36157371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148920-C-T

36157377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148914-T-A

36157385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148906-T-C

36157393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148898-A-G

36157434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148856-A-G

http://identifiers.org/hco/1/GRCh38#36157573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126148723-A-C

http://identifiers.org/hco/1/GRCh38#36157639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126148671-C-A

http://identifiers.org/hco/1/GRCh38#36157657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126148653-C-A

36157819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148505-G-A

36158161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148191-C-G

36158161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148191-C-T

36158162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126148190-G-A

http://identifiers.org/hco/1/GRCh38#36158234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126148144-A-C

http://identifiers.org/hco/1/GRCh38#36158544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126147819-A-C

36158633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126147741-G-C

36158849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126147550-G-A

36159014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126147408-C-T

36159304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126147251-C-T

36159566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126146976-C-G

36160422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126146171-C-G

http://identifiers.org/hco/1/GRCh38#36160434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126146159-C-A

http://identifiers.org/hco/1/GRCh38#36160440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126146152-C-A

36160440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126146152-C-T

36160528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126146081-C-T

36160532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126146077-C-G

36160796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126145836-G-A

36161349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126145387-C-T

36161402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126145332-C-T

36161545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126145188-A-G

36161789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126144998-C-G

36161789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126144998-C-T

36162077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126144809-G-C

36162133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126144769-C-G

36162445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126144451-T-C

36162530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126144376-C-T

http://identifiers.org/hco/1/GRCh38#36162624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126144288-A-C

36163082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126143485-G-A

http://identifiers.org/hco/1/GRCh38#36163213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126143371-A-C

36163332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126143233-G-C

36163622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126142945-A-G

http://identifiers.org/hco/1/GRCh38#36163808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126142764-A-C

36163808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126142764-A-T

36163874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126142697-C-G

http://identifiers.org/hco/1/GRCh38#36164259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126142458-A-C

36164521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126142269-A-G

36164901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126141965-T-A

36164902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126141964-C-T

36166818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126140588-A-G

36167941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126139672-C-G

36168466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126139520-C-T

http://identifiers.org/hco/1/GRCh38#36168595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126139408-A-C

36168595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126139408-A-T

36169726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126138027-G-C

36170375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126136916-A-G

http://identifiers.org/hco/1/GRCh38#36170600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126136517-C-A

36170880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126136247-A-G

36170939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126136191-G-A

http://identifiers.org/hco/1/GRCh38#36171009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126136120-C-A

36171009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126136120-C-G

36171009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126136120-C-T

36171283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126135840-T-C

36171461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126135682-T-C

36171566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126135587-C-G

36171566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126135587-C-T

36171597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135556-G-A

http://identifiers.org/hco/1/GRCh38#36171622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126135534-C-A

36171622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135534-C-G

36171622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135534-C-T

http://identifiers.org/hco/1/GRCh38#36171631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126135525-C-A

36171631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135525-C-G

36171631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135525-C-T

36171659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135492-G-A

36171702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135440-G-C

36171719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135422-G-A

36171719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135422-G-T

http://identifiers.org/hco/1/GRCh38#36171773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126135317-A-C

36171788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135302-G-T

36171801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135289-G-A

36171801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126135289-G-T

http://identifiers.org/hco/1/GRCh38#36171833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126135258-C-A

36171833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126135258-C-T

36171842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126135249-G-A

36171883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126135223-G-A

36171883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126135223-G-T

36171897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126135210-G-A

http://identifiers.org/hco/1/GRCh38#36171919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126135192-A-C

36171919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126135192-A-T

http://identifiers.org/hco/1/GRCh38#36172170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126134952-C-A

36172170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134952-C-T

http://identifiers.org/hco/1/GRCh38#36172184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126134938-C-A

36172212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134894-A-G

36172212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134894-A-T

36172289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134841-T-C

36172289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134841-T-G

36172306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134823-T-C

36172309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134820-A-G

36172375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134750-T-C

http://identifiers.org/hco/1/GRCh38#36172390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126134741-C-A

36172390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134741-C-T

36172392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134739-T-G

36172394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134737-G-A

36172394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126134737-G-T

http://identifiers.org/hco/1/GRCh38#36172698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126134448-C-A

36172698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126134448-C-T

36172728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126134429-G-A

36172728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126134429-G-T

36172884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126134322-C-T

36173364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 126133928-G-A

http://identifiers.org/hco/1/GRCh38#36173367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126133925-C-A

36173367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126133925-C-T

36173564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126133733-G-A

36173564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126133733-G-T

http://identifiers.org/hco/1/GRCh38#36173576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126133711-C-A

36174851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126132471-G-A

36174851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126132471-G-T

http://identifiers.org/hco/1/GRCh38#36175089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126132241-C-A

36175101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126132230-G-A

36175101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126132230-G-C

36175101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126132230-G-T

36175765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131592-G-A

36175820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131537-G-A

http://identifiers.org/hco/1/GRCh38#36176084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126131166-C-A

http://identifiers.org/hco/1/GRCh38#36176094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126131157-A-C

36176094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131157-A-G

36176117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131134-T-C

36176117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131134-T-G

36176119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131132-G-A

36176119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131132-G-T

http://identifiers.org/hco/1/GRCh38#36176163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126131104-C-A

36176163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131104-C-G

36176163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131104-C-T

36176182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126131085-T-C

36176273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: 126130995-G-A

36176273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: 126130995-G-T

http://identifiers.org/hco/1/GRCh38#36176276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126130992-C-A

36176276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: 126130992-C-T

http://identifiers.org/hco/1/GRCh38#36176462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126130806-C-A

36176462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: 126130806-C-T

http://identifiers.org/hco/1/GRCh38#36176474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126130794-A-C

36176474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: 126130794-A-G

http://identifiers.org/hco/1/GRCh38#36176552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126130716-C-A

36176552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: 126130716-C-G

36176552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: 126130716-C-T

36176646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126130638-G-A

36176646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126130638-G-T

36176650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126130634-G-A

36176652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126130632-G-A

36176652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126130632-G-C

36176652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron variant
orthologous variants: 126130632-G-T

36176724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense variant
orthologous variants: 126130536-G-C

http://identifiers.org/hco/1/GRCh38#36176798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126130462-C-A

36176798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: synonymous variant
orthologous variants: 126130462-C-T

http://identifiers.org/hco/1/GRCh38#36176872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126130388-C-A

http://identifiers.org/hco/1/GRCh38#36176979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126130312-C-A

36176979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126130312-C-G

36176979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126130312-C-T

http://identifiers.org/hco/1/GRCh38#36177019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126130284-C-A

36177019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126130284-C-T

36177020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126130283-G-A

36177263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126129981-T-A

36177829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128940-G-A

36177829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128940-G-C

36177829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128940-G-T

36177834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128935-G-A

36177859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128900-C-G

36177859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128900-C-T

http://identifiers.org/hco/1/GRCh38#36177908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126128851-C-A

36177908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126128851-C-T

http://identifiers.org/hco/1/GRCh38#36177976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126128783-C-A

36177976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126128783-C-T

http://identifiers.org/hco/1/GRCh38#36177985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126128774-C-A

http://identifiers.org/hco/1/GRCh38#36178052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126128707-C-A

36178052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126128707-C-T

36178060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126128699-C-T

36178072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126128687-A-G

36178147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126128612-T-C

36178215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128544-G-A

36178215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128544-G-C

36178215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128544-G-T

36178251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128513-C-T

36178264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128499-G-A

36178264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128499-G-C

36178264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128499-G-T

36178268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126128495-G-T

http://identifiers.org/hco/1/GRCh38#36178397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126128331-C-A

36178414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126128314-T-G

36178523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 126128187-G-T

36178612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126128097-G-A

36178612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126128097-G-T

36178619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126128090-G-A

36178619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126128090-G-T

36178646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126128063-A-T

http://identifiers.org/hco/1/GRCh38#36178723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126127989-C-A

36178723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126127989-C-T

36178746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126127966-G-A

36178856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127853-G-A

36178891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127818-G-A

36178891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127818-G-T

36178892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127817-T-C

36178894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127815-C-T

36178930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126127779-G-A

36178930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126127779-G-T

36178954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126127755-G-C

36178954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126127755-G-T

36179051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127660-T-C

36179051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127660-T-G

36179053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127658-G-A

36179053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127658-G-T

36179383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127325-G-T

http://identifiers.org/hco/1/GRCh38#36179457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126127256-C-A

36179457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127256-C-T

36179483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127230-T-C

http://identifiers.org/hco/1/GRCh38#36179496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126127217-C-A

36179496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127217-C-G

36179496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126127217-C-T

http://identifiers.org/hco/1/GRCh38#36179534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126127179-C-A

36179548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126127165-T-A

36179548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126127165-T-C

36179596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126127122-A-G

http://identifiers.org/hco/1/GRCh38#36179599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126127119-C-A

36179599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126127119-C-G

36179599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126127119-C-T

http://identifiers.org/hco/1/GRCh38#36179615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126127100-C-A

36179615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126127100-C-G

36179658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126127065-T-C

36179659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126127064-G-A

36179659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126127064-G-C

36179659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126127064-G-T

36179726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126126997-A-G

36179791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126126935-G-A

36179802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126126925-C-T

36179846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126126880-T-A

36179866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126126860-A-G

36179911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126126815-G-C

36179962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126126764-C-T

36179963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126126763-C-G

36179963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126126763-C-T

36179987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126126739-G-A

36179987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126126739-G-T

36179997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126126729-G-T

36180126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126126593-C-G

36180126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126126593-C-T

36180311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126496-A-G

36180347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126460-A-G

36180362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126442-G-A

36180362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126442-G-T

36180404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126401-T-A

36180630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126182-G-A

36180630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126182-G-T

36180633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126174-G-A

http://identifiers.org/hco/1/GRCh38#36180784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126126028-C-A

36180802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126126010-T-C

http://identifiers.org/hco/1/GRCh38#36180824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25514
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126125988-C-A